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rs41545712

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41545712(G;T)
Make rs41545712(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270044
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41545712
ebirs41545712
HLIrs41545712
Exacrs41545712
Varsomers41545712
Maprs41545712
PheGenIrs41545712
hapmaprs41545712
1000 genomesrs41545712
hgdprs41545712
ensemblrs41545712
gopubmedrs41545712
geneviewrs41545712
scholarrs41545712
googlers41545712
pharmgkbrs41545712
gwascentralrs41545712
openSNPrs41545712
23andMers41545712
23andMe allrs41545712
SNP Nexus

SNPshotrs41545712
SNPdbers41545712
MSV3drs41545712
GWAS Ctlgrs41545712
Max Magnitude0
ClinVar
Risk rs41545712(T;T)
Alt rs41545712(T;T)
Reference rs41545712(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237821C>A
CLNSRC
CLNACC